Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LP Rotate Foot System prosthetic device for fitting lower extremity Recalled by Ossur H / F Due to The threads of the outer tube of the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Ossur H / F directly.
Affected Products
LP Rotate Foot System prosthetic device for fitting lower extremity amputations. -Low profile foot module with adjustable shock absorber and rotation with progressive stiffening -Build height: with male pyramid adapter 145 - 153mm (5 11/16 - 6 ) with female pyramid adapter 153 165mm (6 - 6 1/2 ) -Male pyramid adapter -Female pyramid adapter -Maintenance free, no lubrication required -Maximum weight: 147kg (325lbs) -Available in sizes 22-30
Quantity: 2,194 (1,464 in U.S. and 730 internationally)
Why Was This Recalled?
The threads of the outer tube of the shock module of LP Rotate are too short, resulting in insecure assembly. Use of the product may cause the patient to fall with continued use, as the shock module can become loose from the foot blade.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ossur H / F
Ossur H / F has 29 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report